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31 in total

1. A POSSIBLE AUTOIMMUNE BASIS FOR ADDISON'S DISEASE IN THREE SIBLINGS, ONE WITH IDIOPATHIC HYPOPARATHYROIDISM, PERNICIOUS ANEMIA AND SUPERFICIAL MONILIASIS.

Authors: W HUNG; C J MIGEON; R H PARROTT
Journal: N Engl J Med Date: 1963-09-26 Impact factor: 91.245

2. Familial Addison's disease with spastic paraplegia.

Authors: J N HARRIS-JONES; P G NIXON
Journal: J Clin Endocrinol Metab Date: 1955-06 Impact factor: 5.958

3. Adrenal hypoplasia.

Authors: P G WINQUIST
Journal: Arch Pathol Date: 1961-03

4. Congenital absence of the pituitary gland.

Authors: J D REID
Journal: J Pediatr Date: 1960-05 Impact factor: 4.406

5. [ADDISON'S DISEASE WITH CEREBRAL SCLEROSIS IN CHILDHOOD. A HEREDITARY SYNDROME TRANSMITTED THROUGH CHROMOSOME X?].

Authors: A FANCONI; A PRADER; W ISLER; F LUETHY; R SIEBENMANN
Journal: Helv Paediatr Acta Date: 1963-12

6. Addison's disease in infancy.

Authors: M J ROBINSON; A WILLIAMS
Journal: Arch Dis Child Date: 1956-08 Impact factor: 3.791

7. Changes in the proportion of cell types in the anterior lobe of the human hypophysis during the first 19 years of life.

Authors: A T RASMUSSEN
Journal: Am J Anat Date: 1950-01

8. Congenital adrenal hypoplasia in two infants.

Authors: L H Zondek; T Zondek
Journal: Acta Paediatr Scand Date: 1968-05

Review 9. The adrenal cortex in childhood. 2. Pathological aspects.

Authors: H K Visser
Journal: Arch Dis Child Date: 1966-04 Impact factor: 3.791

10. Congenital adrenal hypoplasia. Report of a case with extreme adrenal hypoplasia and neurohypophyseal aplasia, drawing attention to certain aspects of etiology and classification.

Authors: N KERENYI
Journal: Arch Pathol Date: 1961-03

8 in total

1. Infantile glycerol kinase deficiency--a condition requiring prompt identification. Clinical, biochemical, and morphological findings in two cases.

Authors: A Kohlschütter; H P Willig; D Schlamp; K Kruse; E R McCabe; H J Schäfer; G Beckenkamp; R Rohkamm
Journal: Eur J Pediatr Date: 1987-11 Impact factor: 3.183

Review 2. Hypogonadotropic hypogonadism in subjects with DAX1 mutations.

Authors: Unmesh Jadhav; Rebecca M Harris; J Larry Jameson
Journal: Mol Cell Endocrinol Date: 2011-06-13 Impact factor: 4.102

3. Adrenal hypoplasia congenita with hypogonadotropic hypogonadism: evidence that DAX-1 mutations lead to combined hypothalmic and pituitary defects in gonadotropin production.

Authors: R L Habiby; P Boepple; L Nachtigall; P M Sluss; W F Crowley; J L Jameson
Journal: J Clin Invest Date: 1996-08-15 Impact factor: 14.808

Familial congenital adrenal hypoplasia.