Forwarded from ยฉ๏ธUWORLD Educational objectives
The ratio of plasma aldosterone concentration to plasma renin activity is the preferred initial screening test for primary hyperaldosteronism. Adrenal suppression testing can confirm the diagnosis, and positive tests require further adrenal imaging. Adrenal venous sampling is the most sensitive test for differentiating adrenal adenoma and bilateral adrenal hyperplasia in patients without discrete unilateral adrenal mass on imaging.
๐15โค4
Forwarded from Medical Mnemonics
- Do you want to publish your paper in the High Impact journal?
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๐ท We will proceed with the journal publishing process with our professional team on MCU RESEARCH COLLABORATION
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- Would you like your work to be seen in the best journals?
๐ท We will proceed with the journal publishing process with our professional team on MCU RESEARCH COLLABORATION
๐ป Feel Free to contact admin ๐ @Mohamm_ADs
๐6๐ฅฐ1
A 43-year-old man comes to the physician reporting acute-onset right knee pain. He was diagnosed with diabetes mellitus a year ago and takes metformin. He does not use tobacco, alcohol, or illicit drugs. The patient is in a monogamous relationship. His father also has diabetes. His temperature is 37 C (98.6 F), blood pressure is 134/86 mm Hg, pulse is 86/min, and respirations are 16/min. BMI is 26 kg/m2. Physical examination shows a slightly swollen and tender right knee and mild hepatomegaly. Right knee x-ray reveals chondrocalcinosis and a moderate effusion. Appropriate analgesic is administered for joint pain. Which of the following is the best next step in management of this patient?
A. Anticitrullinated peptide antibodies
B. Antismooth muscle antibodies
C. Liver biopsy
D. Serum iron studies
E. Serum uric acid level
F. Slit-lamp eye examination
A. Anticitrullinated peptide antibodies
B. Antismooth muscle antibodies
C. Liver biopsy
D. Serum iron studies
E. Serum uric acid level
F. Slit-lamp eye examination
๐37โค4๐ฅ3
Case-based MCQ
A 43-year-old man comes to the physician reporting acute-onset right knee pain. He was diagnosed with diabetes mellitus a year ago and takes metformin. He does not use tobacco, alcohol, or illicit drugs. The patient is in a monogamous relationship. Hisโฆ
Clinical manifestations of hereditary hemochromatosis
Skin
Hyperpigmentation (bronze diabetes)
Musculoskeletal
Arthralgia, arthropathy & chondrocalcinosis
Gastrointestinal
Elevated hepatic enzymes with hepatomegaly (early), cirrhosis (later) & increased risk of hepatocellular carcinoma
Endocrine
Diabetes mellitus, secondary hypogonadism & hypothyroidism
Cardiac
Restrictive or dilated cardiomyopathy & conduction abnormalities
Infections
Increased susceptibility to Listeria, Vibrio vulnificus & Yersinia enterocolitica
This patient has acute monoarticular arthritis with chondrocalcinosis (calcified articular cartilage on radiographs), diagnostic of calcium pyrophosphate dihydrate crystal deposition (CPPD) disease (pseudogout). Patients with pseudogout should be evaluated for secondary causes such as hyperparathyroidism, hypothyroidism, and hemochromatosis. Given this patient's recently diagnosed diabetes mellitus and hepatomegaly, hereditary hemochromatosis (HH) is highly likely. HH-induced iron deposition in the synovial fluid appears to promote CPPD. Diabetes in HH appears to be due primarily to loss of insulin secretion and often requires injectable insulin; however, mild or early disease is frequently managed with oral agents.
The initial evaluation of HH includes serum iron studies, which will show increased levels of serum iron, ferritin, and transferrin saturation. The diagnosis can be confirmed with genetic testing for hemochromatosis-associated mutations (eg, HFE). Liver biopsy is not required but may be useful to stage the extent of liver involvement (eg, in patients with significant liver function test abnormalities) or to confirm the diagnosis in patients who have iron studies indicating iron overload but negative results on the classic HFE gene markers (Choice C). Long-term management of hemochromatosis involves serial phlebotomy to deplete excess iron stores.
(Choices A and E) Chondrocalcinosis is not a typical feature of gout or rheumatoid arthritis (which is associated with anticitrullinated peptide antibodies).
(Choice B) Antismooth muscle antibodies are seen in autoimmune hepatitis, which can be associated with other autoimmune disorders including type 1 diabetes mellitus, thyroid disease, and rheumatoid arthritis. Patients may develop a subacute, symmetric polyarthritis involving the small joints, but acute monoarthritis with chondrocalcinosis would not be seen.
(Choice F) Slit-lamp eye examination is helpful in identifying the Kayser-Fleischer rings of Wilson disease. Wilson disease can cause hepatomegaly; however, it typically presents with neuropsychiatric manifestations, and almost all patients are diagnosed before age 35.
Educational objective:
Hereditary hemochromatosis is commonly associated with calcium pyrophosphate dihydrate crystal deposition in joints, leading to chondrocalcinosis, pseudogout, and chronic arthropathy. Patients commonly also have diabetes and liver disease. Diagnosis is suggested by iron overload on serum iron studies and can be confirmed by genetic tests
Skin
Hyperpigmentation (bronze diabetes)
Musculoskeletal
Arthralgia, arthropathy & chondrocalcinosis
Gastrointestinal
Elevated hepatic enzymes with hepatomegaly (early), cirrhosis (later) & increased risk of hepatocellular carcinoma
Endocrine
Diabetes mellitus, secondary hypogonadism & hypothyroidism
Cardiac
Restrictive or dilated cardiomyopathy & conduction abnormalities
Infections
Increased susceptibility to Listeria, Vibrio vulnificus & Yersinia enterocolitica
This patient has acute monoarticular arthritis with chondrocalcinosis (calcified articular cartilage on radiographs), diagnostic of calcium pyrophosphate dihydrate crystal deposition (CPPD) disease (pseudogout). Patients with pseudogout should be evaluated for secondary causes such as hyperparathyroidism, hypothyroidism, and hemochromatosis. Given this patient's recently diagnosed diabetes mellitus and hepatomegaly, hereditary hemochromatosis (HH) is highly likely. HH-induced iron deposition in the synovial fluid appears to promote CPPD. Diabetes in HH appears to be due primarily to loss of insulin secretion and often requires injectable insulin; however, mild or early disease is frequently managed with oral agents.
The initial evaluation of HH includes serum iron studies, which will show increased levels of serum iron, ferritin, and transferrin saturation. The diagnosis can be confirmed with genetic testing for hemochromatosis-associated mutations (eg, HFE). Liver biopsy is not required but may be useful to stage the extent of liver involvement (eg, in patients with significant liver function test abnormalities) or to confirm the diagnosis in patients who have iron studies indicating iron overload but negative results on the classic HFE gene markers (Choice C). Long-term management of hemochromatosis involves serial phlebotomy to deplete excess iron stores.
(Choices A and E) Chondrocalcinosis is not a typical feature of gout or rheumatoid arthritis (which is associated with anticitrullinated peptide antibodies).
(Choice B) Antismooth muscle antibodies are seen in autoimmune hepatitis, which can be associated with other autoimmune disorders including type 1 diabetes mellitus, thyroid disease, and rheumatoid arthritis. Patients may develop a subacute, symmetric polyarthritis involving the small joints, but acute monoarthritis with chondrocalcinosis would not be seen.
(Choice F) Slit-lamp eye examination is helpful in identifying the Kayser-Fleischer rings of Wilson disease. Wilson disease can cause hepatomegaly; however, it typically presents with neuropsychiatric manifestations, and almost all patients are diagnosed before age 35.
Educational objective:
Hereditary hemochromatosis is commonly associated with calcium pyrophosphate dihydrate crystal deposition in joints, leading to chondrocalcinosis, pseudogout, and chronic arthropathy. Patients commonly also have diabetes and liver disease. Diagnosis is suggested by iron overload on serum iron studies and can be confirmed by genetic tests
๐31โค6
A 76-year-old woman comes to the office for evaluation of leukopenia. The patient came to the United States to visit her son a month ago and was seen at an urgent care clinic 2 weeks ago for acute sinusitis, where she was found to have leukopenia. She was prescribed an oral antibiotic, and a repeat blood test was advised. The patient has had 2 episodes of skin infections over the past 3 months. She also has had pain and swelling in the joints of her hands and knees for the past several years. The patient does not use tobacco, alcohol, or illicit drugs. Temperature is 37.2 C (98.9 F), blood pressure is 130/80 mm Hg, and pulse is 74/min. Physical examination shows normal heart and lung sounds, moderate splenomegaly, generalized lymphadenopathy, no sinus tenderness, and well-healing lower extremity ulcerations. The small joints of the hands are swollen and deformed. Laboratory results are as follows:
Hemoglobin 11.8 g/dL
Mean corpuscular volume 92 ยตm3
Platelets 280,000/mm3
Leukocytes 1,800/mm3 (20% neutrophils)
Creatinine 0.8 mg/dL
Calcium 9.2 mg/dL
Erythrocyte sedimentation rate 68 mm/h
HIV serology negative
Additional evaluation of this patient is most likely to reveal which of the following?
A. Anticitrullinated peptide antibodies
B. Decreased vitamin B12 level
C. Hypocellular bone marrow
D. Philadelphia (Ph1) chromosome
E. Serum monoclonal proteins
Hemoglobin 11.8 g/dL
Mean corpuscular volume 92 ยตm3
Platelets 280,000/mm3
Leukocytes 1,800/mm3 (20% neutrophils)
Creatinine 0.8 mg/dL
Calcium 9.2 mg/dL
Erythrocyte sedimentation rate 68 mm/h
HIV serology negative
Additional evaluation of this patient is most likely to reveal which of the following?
A. Anticitrullinated peptide antibodies
B. Decreased vitamin B12 level
C. Hypocellular bone marrow
D. Philadelphia (Ph1) chromosome
E. Serum monoclonal proteins
๐15โค5๐3๐1๐1๐ค1
Case-based MCQ
A 76-year-old woman comes to the office for evaluation of leukopenia. The patient came to the United States to visit her son a month ago and was seen at an urgent care clinic 2 weeks ago for acute sinusitis, where she was found to have leukopenia. She wasโฆ
Felty syndrome
โชClinical features
Rheumatoid arthritis
Severe erosive joint disease & deformity
Rheumatoid nodules
Vasculitis (mononeuritis multiplex, necrotizing skin lesions)
Neutropenia (ANC <2000/ยตL)
Splenomegaly
โชDiagnosis
Anti-CCP & RF are positive in >90% of patients
Markedly elevated ESR, often >85 mm/hr
Peripheral smear & bone marrow biopsy to rule out other causes of neutropenia
ANC = absolute neutrophil count; anti-CCP = anticyclic citrullinated peptide; ESR = erythrocyte sedimentation rate; RF = rheumatoid factor.
This patient with swollen, deformed hand joints and an elevated erythrocyte sedimentation rate likely has untreated inflammatory polyarthritis. The presence of concurrent neutropenia and splenomegaly raise strong suspicion for Felty syndrome, an uncommon but serious complication of long-standing, erosive rheumatoid arthritis (RA).
Felty syndrome is marked by the formation of autoantibodies against neutrophil components and granulocyte colony-stimulating factor, leading to neutropenia (ie, absolute neutrophil count <2,000/mm3) and an increased risk of recurrent bacterial infection (particularly of the skin and sinuses). Neutrophils coated with antibodies are also trapped in the spleen, which usually results in splenomegaly. Most patients also have extraarticular manifestations of RA such as lymphadenopathy, rheumatoid nodules, and/or necrotizing skin lesions.
The diagnosis is made based on clinical features but is supported by the presence of high-titer rheumatoid factor and anticitrullinated peptide antibodies (both of which are usually elevated in RA). Most patients are also HLA-DR4 positive (indicating a genetic susceptibility). Other causes of neutropenia should be ruled out with bone marrow biopsy and peripheral smear prior to establishing the diagnosis. Symptoms generally improve with treatment of the underlying RA.
โชClinical features
Rheumatoid arthritis
Severe erosive joint disease & deformity
Rheumatoid nodules
Vasculitis (mononeuritis multiplex, necrotizing skin lesions)
Neutropenia (ANC <2000/ยตL)
Splenomegaly
โชDiagnosis
Anti-CCP & RF are positive in >90% of patients
Markedly elevated ESR, often >85 mm/hr
Peripheral smear & bone marrow biopsy to rule out other causes of neutropenia
ANC = absolute neutrophil count; anti-CCP = anticyclic citrullinated peptide; ESR = erythrocyte sedimentation rate; RF = rheumatoid factor.
This patient with swollen, deformed hand joints and an elevated erythrocyte sedimentation rate likely has untreated inflammatory polyarthritis. The presence of concurrent neutropenia and splenomegaly raise strong suspicion for Felty syndrome, an uncommon but serious complication of long-standing, erosive rheumatoid arthritis (RA).
Felty syndrome is marked by the formation of autoantibodies against neutrophil components and granulocyte colony-stimulating factor, leading to neutropenia (ie, absolute neutrophil count <2,000/mm3) and an increased risk of recurrent bacterial infection (particularly of the skin and sinuses). Neutrophils coated with antibodies are also trapped in the spleen, which usually results in splenomegaly. Most patients also have extraarticular manifestations of RA such as lymphadenopathy, rheumatoid nodules, and/or necrotizing skin lesions.
The diagnosis is made based on clinical features but is supported by the presence of high-titer rheumatoid factor and anticitrullinated peptide antibodies (both of which are usually elevated in RA). Most patients are also HLA-DR4 positive (indicating a genetic susceptibility). Other causes of neutropenia should be ruled out with bone marrow biopsy and peripheral smear prior to establishing the diagnosis. Symptoms generally improve with treatment of the underlying RA.
๐21๐ฅฐ3๐2๐ฅ1
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๐2
Forwarded from Medical Mnemonics
๐งฉ Medical Mnemonics
๐ฎโ โ๐ผโโ๐ฆโโ๐นโโ๐จโโ๐ญโ โ๐ฉโโ๐ชโโ๐ฆโโ๐นโโ๐ญโ โ๐ฝ
๐ชง ๐ nfectious (encephalitis, meningitis, UTI)
๐ชง ๐ ฆithdrawal (alcohol, benzodiazepines)
๐ชง ๐ cute metabolic disorder (electrolyte imbalance)
๐ชง ๐ ฃrauma (head injury, postoperative)
๐ชง ๐ NS pathology (stroke, hemorrhage, tumor)
๐ชง ๐ ypoxia (anemia, cardiac failure)
๐ชง ๐ eficiencies (vitamin B12, folic acid, thiamine)
๐ชง ๐ ndocrinopathies (thyroid, glucose)
๐ชง ๐ cute vascular (shock, vasculitis,
hypertension)
๐ชง ๐ ฃoxins, substance use, medications
๐ชง ๐ eavy metals (arsenic, lead, mercury)
#psychiatry
ใฐใฐใฐใฐใฐใฐใฐใฐใฐใฐใฐ
ยฉMedical Mnemonics
Causes of delirium๐ฎโ โ๐ผโโ๐ฆโโ๐นโโ๐จโโ๐ญโ โ๐ฉโโ๐ชโโ๐ฆโโ๐นโโ๐ญโ โ๐ฝ
๐ชง ๐ nfectious (encephalitis, meningitis, UTI)
๐ชง ๐ ฆithdrawal (alcohol, benzodiazepines)
๐ชง ๐ cute metabolic disorder (electrolyte imbalance)
๐ชง ๐ ฃrauma (head injury, postoperative)
๐ชง ๐ NS pathology (stroke, hemorrhage, tumor)
๐ชง ๐ ypoxia (anemia, cardiac failure)
๐ชง ๐ eficiencies (vitamin B12, folic acid, thiamine)
๐ชง ๐ ndocrinopathies (thyroid, glucose)
๐ชง ๐ cute vascular (shock, vasculitis,
hypertension)
๐ชง ๐ ฃoxins, substance use, medications
๐ชง ๐ eavy metals (arsenic, lead, mercury)
#psychiatry
ใฐใฐใฐใฐใฐใฐใฐใฐใฐใฐใฐ
ยฉMedical Mnemonics
๐13
Forwarded from Medical Mnemonics
๐งฉ Medical Mnemonics
Modified Alvarado score for diagnosis of appendicitis
๐ ๐จ๐ฆ โ๐ฒโโ๐ดโโ๐ณโโ๐นโโ๐ทโโ๐ชโโ๐ฆโโ๐ฑโ
โ๐ igration ๐ขf pain to right lower quadrant (1 point)
โ๐กausea and vomiting (1 point)
โ๐งenderness in right lower quadrant (2 points)
โ๐ฅebound tenderness (1 point)
โ๐levated temperature (1 point)
โ๐norexia (1 point)
โ๐eukocytosis >10 ร 10โน/liter (2 points)
- Score of โฅ4 indicates that the patient should be further evaluated for appendicitis.
#surgery
ใฐใฐใฐใฐใฐใฐใฐใฐใฐใฐใฐ
ยฉMedical Mnemonics
Modified Alvarado score for diagnosis of appendicitis
๐ ๐จ๐ฆ โ๐ฒโโ๐ดโโ๐ณโโ๐นโโ๐ทโโ๐ชโโ๐ฆโโ๐ฑโ
โ๐ igration ๐ขf pain to right lower quadrant (1 point)
โ๐กausea and vomiting (1 point)
โ๐งenderness in right lower quadrant (2 points)
โ๐ฅebound tenderness (1 point)
โ๐levated temperature (1 point)
โ๐norexia (1 point)
โ๐eukocytosis >10 ร 10โน/liter (2 points)
- Score of โฅ4 indicates that the patient should be further evaluated for appendicitis.
#surgery
ใฐใฐใฐใฐใฐใฐใฐใฐใฐใฐใฐ
ยฉMedical Mnemonics
๐14โค1
Forwarded from Medical Mnemonics
๐งฉ Medical Mnemonics
Hypokalemia
Eid Mubarak ๐บ๐ ๐๐
โกEnteric losses ( diarrhea)
โกInsulin excess, Increase of Glucocorticoid (Cushing's, exogenous steroids, ectopic ACTH), Increased sweat losses
โกDialysis, Decrease of body temperature (hypothermia)
โกMagnesium depletion
โกUrinary losses(Diuretics)
โกฮฒ-adrenergic activity, Bartter's or Gitelman's syndrome
โกAlkalosis, Amphotericin B
โกRTA types I and II
โกAldosteronism
โกKetoacidosis
#nephrology
ใฐใฐใฐใฐใฐใฐใฐใฐใฐใฐใฐ
ยฉMedical Mnemonics
Hypokalemia
causes Eid Mubarak ๐บ๐ ๐๐
โกEnteric losses ( diarrhea)
โกInsulin excess, Increase of Glucocorticoid (Cushing's, exogenous steroids, ectopic ACTH), Increased sweat losses
โกDialysis, Decrease of body temperature (hypothermia)
โกMagnesium depletion
โกUrinary losses(Diuretics)
โกฮฒ-adrenergic activity, Bartter's or Gitelman's syndrome
โกAlkalosis, Amphotericin B
โกRTA types I and II
โกAldosteronism
โกKetoacidosis
#nephrology
ใฐใฐใฐใฐใฐใฐใฐใฐใฐใฐใฐ
ยฉMedical Mnemonics
โค25๐6๐ฅฐ1
Forwarded from Medical Mnemonics
๐งฉ Medical Mnemonics
Differential diagnosis of elevated serum aminotransferases
๐ โ๐ฆโโ๐งโโ๐จโโ๐ฉโโ๐ชโโ๐ซโโ๐ฌโโ๐ญโโ๐ฎโ
๐ชถ ๐utoimmune hepatitis, ๐drenal insufficiency, ๐norexia nervosa
๐ชถ Hepatitis ๐
๐ชถ Hepatitis ๐, ๐eliac disease
๐ชถ ๐rugs or toxins
๐ชถ ๐thanol
๐ชถ ๐atty liver
๐ชถ ๐enetic disorders (Wilson disease, Hemochromatosis, Alpha-1 antitrypsin deficiency)
๐ชถ ๐emodynamic disorders (CHF and MI)
๐ชถ ๐nfiltration of the liver by malignancy, ๐njury to muscle (strenuous exercise, myopathy)
#gastroenterology
ใฐใฐใฐใฐใฐใฐใฐใฐใฐใฐใฐ
ยฉMedical Mnemonics
Differential diagnosis of elevated serum aminotransferases
๐ โ๐ฆโโ๐งโโ๐จโโ๐ฉโโ๐ชโโ๐ซโโ๐ฌโโ๐ญโโ๐ฎโ
๐ชถ ๐utoimmune hepatitis, ๐drenal insufficiency, ๐norexia nervosa
๐ชถ Hepatitis ๐
๐ชถ Hepatitis ๐, ๐eliac disease
๐ชถ ๐rugs or toxins
๐ชถ ๐thanol
๐ชถ ๐atty liver
๐ชถ ๐enetic disorders (Wilson disease, Hemochromatosis, Alpha-1 antitrypsin deficiency)
๐ชถ ๐emodynamic disorders (CHF and MI)
๐ชถ ๐nfiltration of the liver by malignancy, ๐njury to muscle (strenuous exercise, myopathy)
#gastroenterology
ใฐใฐใฐใฐใฐใฐใฐใฐใฐใฐใฐ
ยฉMedical Mnemonics
๐10โค4
Forwarded from Medical Mnemonics
On MCU RESEARCH COLLABORATION, we provide you:
- Language revision
- Scientific Editing
- Journal Selection
- Submitting the manuscript
- Guide to dealing with Journals
๐ And Much More!
๐ชฉ Feel Free to contact admin ๐ @Mohamm_ADs
- Language revision
- Scientific Editing
- Journal Selection
- Submitting the manuscript
- Guide to dealing with Journals
๐ And Much More!
๐ชฉ Feel Free to contact admin ๐ @Mohamm_ADs
๐1
Forwarded from Medical Mnemonics
๐งฉ Medical Mnemonics
Learn ๐ซง SOAP BUBBLE appearance in Giant cell tumor of bone by #visual_mnemonics.
๐ป Join us in the official Instagram page: Online Medical School
#radiology
ใฐใฐใฐใฐใฐใฐใฐใฐใฐใฐใฐ
ยฉMedical Mnemonics
Learn ๐ซง SOAP BUBBLE appearance in Giant cell tumor of bone by #visual_mnemonics.
๐ป Join us in the official Instagram page: Online Medical School
#radiology
ใฐใฐใฐใฐใฐใฐใฐใฐใฐใฐใฐ
ยฉMedical Mnemonics
๐6โค1
Forwarded from EDL Backup Channel
โ ๐ ๐๐๐๐ ๐๐๐๐ ๐๐๐๐ ๐
๐๐ ๐ ๐๐๐๐๐ ๐๐๐ ! โคต
1. ๐งฉ ๐ ๐๐๐๐๐๐ ๐ ๐ก๐๐ ๐ข๐ก๐๐๐ฆ (๐๐๐๐ฅ๐ก ๐๐๐ฆ๐๐๐ฌ)
2. ๐๐๐ฆ๐ - ๐๐๐ฆ๐๐ ๐ ๐๐ค๐ฆ ๐ฏ
3. ๐จ๐ฆ ๐ ๐๐๐ค๐ ๐ฃ๐ฅ๐๐ฃ๐๐ฅ๐๐ง๐๐ข๐ก
4. ๐ฉบ ๐๐๐ ๐ ๐๐๐๐๐ข๐ฆ (๐ ๐๐๐๐๐๐ ๐๐ข๐ข๐๐ฆ ๐๐ก๐ ๐๐๐ก๐๐ฆ)
5. ๐ ๐๐๐ ๐ฃ๐๐๐ฅ๐
6. ๐ ๐ข๐ก๐๐๐ก๐ ๐ ๐๐๐๐๐๐ ๐ฆ๐๐๐ข๐ข๐
7. ๐ฅ๐๐ฆ๐๐๐๐ก๐๐ฌ ๐๐ก ๐๐๐ฅ๐ ๐๐ก๐ฌ ๐ฉ๐ช
8. ๐ฃ๐ฅ๐๐๐ง๐๐๐ ๐๐ก ๐๐จ๐ฆ๐ง๐ฅ๐๐๐๐ ๐ฆ๐บ
9. ๐ ๐๐๐ฆ & ๐ฅ๐๐ฆ๐๐๐๐ก๐๐ฌ ๐๐ก ๐๐ง๐๐๐ฌ ๐ฎ๐น
10. ๐ฅ๐๐ฆ๐๐๐๐ก๐๐ฌ ๐๐ก ๐จ๐ ๐ฌ๐ง
11. ๐ฅ๐๐ฆ๐๐๐๐ก๐๐ฌ ๐๐ก ๐จ๐ฆ ๐บ๐ธ
12. ๐ฅ๐๐ฆ๐๐๐๐ก๐๐ฌ ๐๐ก ๐๐๐ก๐๐๐ ๐จ๐ฆ
13. ๐๐ฅ๐๐ก๐๐ ๐ ๐๐๐๐๐๐ ๐๐ข๐ข๐๐ฆ ๐ซ๐ท
14. ๐๐๐ฅ๐ ๐๐ก ๐ ๐๐๐๐๐๐ ๐๐ข๐ข๐๐ฆ ๐ฉ๐ช
15. ๐ ๐๐๐๐๐๐ ๐ฅ๐๐ฆ๐๐๐ฅ๐๐ ๐
16. ๐ธ ๐๐๐ฅ๐ ๐๐ง๐ข๐๐ข๐๐ฌ ๐๐ง๐๐๐ฆ
17. ๐ข๐๐ง ๐ฃ๐ฅ๐๐ฃ๐๐ฅ๐๐ง๐๐ข๐ก ๐ก
18. ๐ ๐๐๐๐๐๐ ๐๐ ๐๐ญ๐ข๐ก ๐
19. ๐ ๐๐๐๐๐๐ข๐จ๐ก๐ง - ๐ ๐๐๐๐๐๐ ๐๐๐๐ข๐จ๐ก๐ง ๐
20. ๐ ๐จ๐ช๐ข๐ฅ๐๐ ๐๐๐จ๐๐๐ง๐๐ข๐ก๐๐ ๐ข๐๐๐๐๐ง๐๐ฉ๐๐ฆ
1. ๐งฉ ๐ ๐๐๐๐๐๐ ๐ ๐ก๐๐ ๐ข๐ก๐๐๐ฆ (๐๐๐๐ฅ๐ก ๐๐๐ฆ๐๐๐ฌ)
2. ๐๐๐ฆ๐ - ๐๐๐ฆ๐๐ ๐ ๐๐ค๐ฆ ๐ฏ
3. ๐จ๐ฆ ๐ ๐๐๐ค๐ ๐ฃ๐ฅ๐๐ฃ๐๐ฅ๐๐ง๐๐ข๐ก
4. ๐ฉบ ๐๐๐ ๐ ๐๐๐๐๐ข๐ฆ (๐ ๐๐๐๐๐๐ ๐๐ข๐ข๐๐ฆ ๐๐ก๐ ๐๐๐ก๐๐ฆ)
5. ๐ ๐๐๐ ๐ฃ๐๐๐ฅ๐
6. ๐ ๐ข๐ก๐๐๐ก๐ ๐ ๐๐๐๐๐๐ ๐ฆ๐๐๐ข๐ข๐
7. ๐ฅ๐๐ฆ๐๐๐๐ก๐๐ฌ ๐๐ก ๐๐๐ฅ๐ ๐๐ก๐ฌ ๐ฉ๐ช
8. ๐ฃ๐ฅ๐๐๐ง๐๐๐ ๐๐ก ๐๐จ๐ฆ๐ง๐ฅ๐๐๐๐ ๐ฆ๐บ
9. ๐ ๐๐๐ฆ & ๐ฅ๐๐ฆ๐๐๐๐ก๐๐ฌ ๐๐ก ๐๐ง๐๐๐ฌ ๐ฎ๐น
10. ๐ฅ๐๐ฆ๐๐๐๐ก๐๐ฌ ๐๐ก ๐จ๐ ๐ฌ๐ง
11. ๐ฅ๐๐ฆ๐๐๐๐ก๐๐ฌ ๐๐ก ๐จ๐ฆ ๐บ๐ธ
12. ๐ฅ๐๐ฆ๐๐๐๐ก๐๐ฌ ๐๐ก ๐๐๐ก๐๐๐ ๐จ๐ฆ
13. ๐๐ฅ๐๐ก๐๐ ๐ ๐๐๐๐๐๐ ๐๐ข๐ข๐๐ฆ ๐ซ๐ท
14. ๐๐๐ฅ๐ ๐๐ก ๐ ๐๐๐๐๐๐ ๐๐ข๐ข๐๐ฆ ๐ฉ๐ช
15. ๐ ๐๐๐๐๐๐ ๐ฅ๐๐ฆ๐๐๐ฅ๐๐ ๐
16. ๐ธ ๐๐๐ฅ๐ ๐๐ง๐ข๐๐ข๐๐ฌ ๐๐ง๐๐๐ฆ
17. ๐ข๐๐ง ๐ฃ๐ฅ๐๐ฃ๐๐ฅ๐๐ง๐๐ข๐ก ๐ก
18. ๐ ๐๐๐๐๐๐ ๐๐ ๐๐ญ๐ข๐ก ๐
19. ๐ ๐๐๐๐๐๐ข๐จ๐ก๐ง - ๐ ๐๐๐๐๐๐ ๐๐๐๐ข๐จ๐ก๐ง ๐
20. ๐ ๐จ๐ช๐ข๐ฅ๐๐ ๐๐๐จ๐๐๐ง๐๐ข๐ก๐๐ ๐ข๐๐๐๐๐ง๐๐ฉ๐๐ฆ
๐6โค2๐1๐1
Forwarded from Medical Mnemonics
- Do you want to publish your paper in the High Impact journal?
- Would you like your work to be seen in the best journals?
๐ท We will proceed with the journal publishing process with our professional team on MCU RESEARCH COLLABORATION
๐ป Feel Free to contact admin ๐ @Mohamm_ADs
- Would you like your work to be seen in the best journals?
๐ท We will proceed with the journal publishing process with our professional team on MCU RESEARCH COLLABORATION
๐ป Feel Free to contact admin ๐ @Mohamm_ADs
โค5